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| Cross-sectional case-control studies  

This study aimed to investigate the factors affecting the unwillingness of physicians involved in epilepsy care to continue telemedicine during the…

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| Cross-sectional case-control studies  

The objective of this case-control study was to assess risk factors for persistent neuropathic pain in subjects recovered from COVID-19 and to study…

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| Cross-sectional case-control studies  

Apolipoprotein E ε4 allele (APOE4) has been shown to associate with increased susceptibility to SARS-CoV-2 infection and COVID-19 mortality in some…

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| Cross-sectional case-control studies  

The objective of this article was to study the longitudinal seizure outcomes of people with epilepsy (PWE) following the acute and chronic phases of…

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| Cross-sectional case-control studies  

The objective of this study was to describe cerebrovascular, neuropathic and autonomic features of post-acute sequelae of COVID-19 (PASC). This…

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| Cross-sectional case-control studies  

In Switzerland, the COVID-19 incidence during the first pandemic wave was high. In this article the authors aimed to assess the association of the…

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| Cross-sectional case-control studies  

Creutzfeldt-Jakob disease (CJD) is lethal and transmissible. In this article the authors assessed the impact of the COVID-19 pandemic on UK CJD…

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| Cross-sectional case-control studies  

Cerebral Venous Sinus Thrombosis (CVST) as a part of the thrombosis and thrombocytopenia syndrome is a rare adverse drug reaction of SARS-CoV-2…

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| Cross-sectional case-control studies  

Stroke management during the COVID-19 outbreak: challenges and results of a hub-center in Lombardy, Italy

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| Cross-sectional case-control studies  

Headache during SARS-CoV-2 infection as an early symptom associated with a more benign course of disease: a case-control study

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| Cross-sectional case-control studies  

Sleep apnoea is a risk factor for severe COVID-19

 

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| Cross-sectional case-control studies  

Central and peripheral nervous system complications of COVID-19: a prospective tertiary center cohort with 3-month follow-up

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